SE449496B - Vattenhaltigt gel fri fran elektroendosmos och forfarande for dess framstellning - Google Patents
Vattenhaltigt gel fri fran elektroendosmos och forfarande for dess framstellningInfo
- Publication number
- SE449496B SE449496B SE8000966A SE8000966A SE449496B SE 449496 B SE449496 B SE 449496B SE 8000966 A SE8000966 A SE 8000966A SE 8000966 A SE8000966 A SE 8000966A SE 449496 B SE449496 B SE 449496B
- Authority
- SE
- Sweden
- Prior art keywords
- agarose
- water
- weight
- purified
- amount
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 10
- 238000002360 preparation method Methods 0.000 title claims 3
- 229920000936 Agarose Polymers 0.000 claims description 59
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 38
- 239000000463 material Substances 0.000 claims description 36
- 229920001971 elastomer Polymers 0.000 claims description 30
- 238000005370 electroosmosis Methods 0.000 claims description 27
- 239000000203 mixture Substances 0.000 claims description 27
- 229920000161 Locust bean gum Polymers 0.000 claims description 15
- 239000000711 locust bean gum Substances 0.000 claims description 15
- 235000010420 locust bean gum Nutrition 0.000 claims description 15
- 238000001155 isoelectric focusing Methods 0.000 claims description 11
- 229920002907 Guar gum Polymers 0.000 claims description 10
- 239000000665 guar gum Substances 0.000 claims description 10
- 235000010417 guar gum Nutrition 0.000 claims description 10
- 229960002154 guar gum Drugs 0.000 claims description 10
- 229920002307 Dextran Polymers 0.000 claims description 9
- 239000002245 particle Substances 0.000 claims description 6
- 239000008247 solid mixture Substances 0.000 claims description 6
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 5
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 4
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims 1
- 239000000499 gel Substances 0.000 description 44
- 239000000243 solution Substances 0.000 description 33
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 238000010438 heat treatment Methods 0.000 description 7
- 229920001817 Agar Polymers 0.000 description 6
- 102000004169 proteins and genes Human genes 0.000 description 6
- 108090000623 proteins and genes Proteins 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
- 238000009835 boiling Methods 0.000 description 5
- 239000000416 hydrocolloid Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 239000000872 buffer Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920002401 polyacrylamide Polymers 0.000 description 4
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 150000007942 carboxylates Chemical group 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 239000012634 fragment Substances 0.000 description 3
- 238000001879 gelation Methods 0.000 description 3
- 150000004676 glycans Chemical class 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 229920001282 polysaccharide Polymers 0.000 description 3
- 239000005017 polysaccharide Substances 0.000 description 3
- 102000009027 Albumins Human genes 0.000 description 2
- 108010088751 Albumins Proteins 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000011543 agarose gel Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000005119 centrifugation Methods 0.000 description 2
- 239000013256 coordination polymer Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 239000012153 distilled water Substances 0.000 description 2
- 238000001962 electrophoresis Methods 0.000 description 2
- 230000007062 hydrolysis Effects 0.000 description 2
- 238000006460 hydrolysis reaction Methods 0.000 description 2
- 125000003010 ionic group Chemical group 0.000 description 2
- 229920000609 methyl cellulose Polymers 0.000 description 2
- 239000001923 methylcellulose Substances 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- HKJKONMZMPUGHJ-UHFFFAOYSA-N 4-amino-5-hydroxy-3-[(4-nitrophenyl)diazenyl]-6-phenyldiazenylnaphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC2=CC(S(O)(=O)=O)=C(N=NC=3C=CC=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 HKJKONMZMPUGHJ-UHFFFAOYSA-N 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- 102000008100 Human Serum Albumin Human genes 0.000 description 1
- 108091006905 Human Serum Albumin Proteins 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920005654 Sephadex Polymers 0.000 description 1
- 239000012507 Sephadex™ Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000007982 barbital buffer Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 239000003729 cation exchange resin Substances 0.000 description 1
- 239000011362 coarse particle Substances 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000012362 glacial acetic acid Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 238000004255 ion exchange chromatography Methods 0.000 description 1
- 238000002218 isotachophoresis Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229930014626 natural product Natural products 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000012460 protein solution Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000012192 staining solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000012085 test solution Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000012800 visualization Methods 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
- G01N27/44752—Controlling the zeta potential, e.g. by wall coatings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L5/00—Compositions of polysaccharides or of their derivatives not provided for in groups C08L1/00 or C08L3/00
- C08L5/12—Agar or agar-agar, i.e. mixture of agarose and agaropectin; Derivatives thereof
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Physics & Mathematics (AREA)
- Polymers & Plastics (AREA)
- Analytical Chemistry (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Electrochemistry (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Colloid Chemistry (AREA)
- Medicinal Preparation (AREA)
- Jellies, Jams, And Syrups (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/010,033 US4290911A (en) | 1979-02-07 | 1979-02-07 | Agarose composition, aqueous gel and method of making same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SE8000966L SE8000966L (sv) | 1980-08-08 |
| SE449496B true SE449496B (sv) | 1987-05-04 |
Family
ID=21743460
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8000966A SE449496B (sv) | 1979-02-07 | 1980-02-06 | Vattenhaltigt gel fri fran elektroendosmos och forfarande for dess framstellning |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US4290911A (zh) |
| JP (1) | JPS55110946A (zh) |
| CA (1) | CA1140833A (zh) |
| DE (1) | DE3004526A1 (zh) |
| DK (1) | DK158587C (zh) |
| ES (1) | ES8300789A3 (zh) |
| FR (1) | FR2448553A1 (zh) |
| GB (1) | GB2042571B (zh) |
| SE (1) | SE449496B (zh) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59126236A (ja) * | 1983-01-08 | 1984-07-20 | Fuji Photo Film Co Ltd | 電気泳動用媒体 |
| GB8513152D0 (en) * | 1985-05-24 | 1985-06-26 | Ciba Geigy Ag | Diagnostic strips |
| US4997537A (en) * | 1986-10-21 | 1991-03-05 | Northeastern University | High performance microcapillary gel electrophoresis |
| US5665216A (en) * | 1986-10-21 | 1997-09-09 | Northeastern University | Capillary column for high performance electrophoretic separation and detection of SDS proteins and system and using the same |
| US4999340A (en) * | 1988-08-04 | 1991-03-12 | Board Of Regents, The University Of Texas System | Rehydratable agarose gels |
| ATE144727T1 (de) * | 1989-01-13 | 1996-11-15 | Fmc Corp | Polysaccharid-trenngele und gelsysteme für elektrophorese unter verwendung von sammelgel |
| US4925545A (en) * | 1989-01-31 | 1990-05-15 | Amest, Inc. | Method of generating pH functions in electrophoresis and isoelectric focusing |
| US4983268A (en) * | 1989-08-03 | 1991-01-08 | Fmc Corporation | High gel strength low electroendosmosis agarose |
| IL95429A (en) * | 1989-09-15 | 1997-09-30 | Organogenesis | Living tissue equivalents comprising hydrated collagen lattice and a collagen gel and their production |
| US5230832A (en) * | 1991-01-24 | 1993-07-27 | Brandeis University | Galactomannan-agarose binary gel for nucleic acid electrophoresis |
| US6162906A (en) * | 1991-08-08 | 2000-12-19 | Fmc Corporation | Clarified konjac glucomannan |
| US5371208A (en) * | 1992-12-30 | 1994-12-06 | Guest Elchrom Scientific Ltd. | Preparation of cross-linked linear polysaccharide polymers as gels for electrophoresis |
| WO1995016910A1 (en) * | 1993-12-17 | 1995-06-22 | Perkin-Elmer Corporation | Uncharged polymers for separation of biomolecules by capillary electrophoresis |
| US6358385B1 (en) | 1993-12-17 | 2002-03-19 | The Perkin-Elmer Corporation | Polymers for separation of biomolecules by capillary electrophoresis |
| US8071133B2 (en) * | 2001-08-20 | 2011-12-06 | Stiefel Laboratories, Inc. | Oral dosage forms of water insoluble drugs and methods of making the same |
| US20040115266A1 (en) * | 2002-02-01 | 2004-06-17 | Namburi Ranga Raju | Oral itraconazole formulations and methods of making the same |
| US20080140106A1 (en) * | 2006-12-12 | 2008-06-12 | Kimberly-Clark Worldwide, Inc. | Enhanced cuff sealing for endotracheal tubes |
| US9388252B2 (en) * | 2014-02-17 | 2016-07-12 | Aurelien Forget | Methods for purifying polysaccharides and pharmaceutical compositions and medical devices containing the same |
| CN103910811A (zh) * | 2014-04-02 | 2014-07-09 | 华侨大学 | 一种低电内渗琼脂糖的制备方法 |
| CN106770412A (zh) * | 2016-11-29 | 2017-05-31 | 广东海洋大学 | 一种明胶凝冻强度的快速测定方法 |
| JP7072830B2 (ja) * | 2017-07-26 | 2022-05-23 | 国立大学法人広島大学 | 高分離能を有する電気泳動用ゲルの製造方法およびその製造キット |
| JP6966071B2 (ja) * | 2017-11-29 | 2021-11-10 | 国立大学法人広島大学 | ゲル分離能向上剤の製造方法およびゲル分離能向上剤の利用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2508726A (en) * | 1946-06-27 | 1950-05-23 | Gen Mills Inc | Precipitation of mannogalactans and glucomannans from aqueous sols |
| US2466146A (en) * | 1947-04-12 | 1949-04-05 | Krim Ko Corp | Edible gelling composition containing irish moss extract, locust bean gum, and an edible salt |
| US3527712A (en) * | 1967-03-07 | 1970-09-08 | Marine Colloids Inc | Dried agarose gel,method of preparation thereof,and production of aqueous agarose gel |
| US3984298A (en) * | 1970-12-28 | 1976-10-05 | Haber Instruments, Incorporated | Electromolecular propulsion in semiconductive media |
| US3767787A (en) * | 1971-10-07 | 1973-10-23 | H Segal | Retarded vaporization compositions and method for making |
| SE358563B (zh) * | 1971-12-13 | 1973-08-06 | Pharmacia Fine Chemicals Ab |
-
1979
- 1979-02-07 US US06/010,033 patent/US4290911A/en not_active Expired - Lifetime
-
1980
- 1980-01-10 CA CA000343435A patent/CA1140833A/en not_active Expired
- 1980-02-05 FR FR8002472A patent/FR2448553A1/fr active Granted
- 1980-02-06 JP JP1255580A patent/JPS55110946A/ja active Granted
- 1980-02-06 GB GB8003898A patent/GB2042571B/en not_active Expired
- 1980-02-06 SE SE8000966A patent/SE449496B/sv not_active IP Right Cessation
- 1980-02-06 DK DK051180A patent/DK158587C/da active
- 1980-02-07 DE DE19803004526 patent/DE3004526A1/de active Granted
-
1981
- 1981-11-20 ES ES507322A patent/ES8300789A3/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| ES507322A0 (es) | 1982-09-01 |
| GB2042571B (en) | 1983-04-13 |
| DK158587B (da) | 1990-06-11 |
| US4290911A (en) | 1981-09-22 |
| JPS6129664B2 (zh) | 1986-07-08 |
| FR2448553A1 (fr) | 1980-09-05 |
| CA1140833A (en) | 1983-02-08 |
| GB2042571A (en) | 1980-09-24 |
| DE3004526C2 (zh) | 1989-02-02 |
| DK51180A (da) | 1980-08-08 |
| JPS55110946A (en) | 1980-08-27 |
| DK158587C (da) | 1990-11-05 |
| ES8300789A3 (es) | 1982-09-01 |
| FR2448553B1 (zh) | 1984-01-13 |
| SE8000966L (sv) | 1980-08-08 |
| DE3004526A1 (de) | 1980-08-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| SE449496B (sv) | Vattenhaltigt gel fri fran elektroendosmos och forfarande for dess framstellning | |
| Bernardin et al. | Preparation and characterization of α-gliadin | |
| Gratzer et al. | Properties of the High‐Molecular‐Weight Protein (Spectrin) from Human‐Erythrocyte Membranes | |
| US4983268A (en) | High gel strength low electroendosmosis agarose | |
| Butzow et al. | Physical chemical studies on the age changes in rat tail tendon collagen | |
| Kohyama et al. | Effects of protein composition on gelation of mixtures containing soybean 7S and 11S globulins | |
| Guido et al. | Phase separation effects in the rheology of aqueous solutions of hydroxypropylcellulose | |
| US3335127A (en) | Fractionation of mixtures of agarose and agaropectin | |
| Ciferri et al. | Phase separation of poly-L-proline in salt solutions | |
| EP0027533B1 (de) | Photographische Materialien, Verfahren zu ihrer Herstellung, ihre Verwendung und die Verwendung von Gelatinen | |
| Salt et al. | Factors influencing protein structure during acid precipitation: a study of soya proteins | |
| Hoagland | Acylated β-caseins. Effect of alkyl group size on calcium ion sensitivity and on aggregation | |
| You et al. | Interactions between hsian-tsao gum and chitosan in aqueous solution | |
| Sukan et al. | Application of the plastein reaction to caseins and to skim-milk powder: II. Chemical and physical properties of the plasteins and the mechanism of plastein formation | |
| EP0025494B1 (de) | Verfahren zur Herstellung von Gelatine | |
| Clark et al. | The application of polyethylene glycol solubility-concentration gradients in plant virus research | |
| Bernengo et al. | Intermolecular interaction studies on native and enzyme-treated acid-soluble collagen | |
| Elfak et al. | The effect of casein on the viscosity of solutions of hydrocolloids | |
| Scallet | Zein Solutions as Association—Dissociation Systems1 | |
| Holme | Characterization studies on the soluble proteins and pentosans of cake flour | |
| Burley | Isolation and properties of a low-molecular-weight protein (apovitellenin I) from the high-lipid lipoprotein of emu egg yolk | |
| McKenzie et al. | Studies of Casein. I. Some Observations on the Heterogeneity of Casein Fractions | |
| Seifert et al. | Characterization of gliadin-galactomannan incubation mixtures by analytical ultracentrifugation—Part I. Sedimentation velocity | |
| Bennett | Behavior of adsorbed protein in cane sugar juice | |
| Shyluk | Poly (1, 2‐dimethyl‐5‐vinylpyridinium methyl sulfate). Part II. Polymer properties |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| NAL | Patent in force |
Ref document number: 8000966-5 Format of ref document f/p: F |
|
| NUG | Patent has lapsed |
Ref document number: 8000966-5 Format of ref document f/p: F |